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Anaerobic dissolved As(III) removal from metalpolluted waters by cathode-stabilized Fe(III)- oxyhydroxides.

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F23%3A00571472" target="_blank" >RIV/60077344:_____/23:00571472 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/60076658:12310/23:43907569 RIV/00025798:_____/23:10168739

  • Výsledek na webu

    <a href="https://pubs.rsc.org/en/content/articlelanding/2023/EW/D2EW00844K" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2023/EW/D2EW00844K</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/d2ew00844k" target="_blank" >10.1039/d2ew00844k</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Anaerobic dissolved As(III) removal from metalpolluted waters by cathode-stabilized Fe(III)- oxyhydroxides.

  • Popis výsledku v původním jazyce

    A bioelectrochemical system (BES) to efficiently induce arsenite scavenging from anoxic waters is yet to be developed. Here we examined to what extent the presence of redox reactive humic substances derivatives and reactive nitrogen species interferes with the bioelectrochemically induced immobilization of As(iii) by Fe(iii) oxyhydroxides. Insights from extracellular electron transfer to insoluble minerals by a strain of Geobacter sp. were acquired and integrated with data from acetate utilization. We furthered our interpretations with in situ synchrotron-based analyses of experimentally precipitated biominerals. Geobacter sp. cells interacting with cathodes used oxidized humic substance derivatives as electron shuttles which fostered the partial reduction of Fe(iii), thus promoting the scavenging of As(iii) oxyanions. The oxyanions became immobilized in the reactive surfaces of FeOOH within mineral aggregates, where they were readily oxidized presumably as the result of related Fenton-like reactions. An experiment lacking humic derivatives fueled the formation of bacterial-mineral networks. These networks fostered short-range electron transfer mechanisms that initially promoted biotic amorphous ferrihydrite aggregation. The early ferrihydrite aggregates exhibited a decreased As(iii) scavenging capacity. In the presence of both humic derivatives and ammonium, the proposed BES was proven more effective in removing As(iii) from solution and despite elevated competing phosphate levels. In the presence of reactive N species alone, stabilization of Fe(iii) and microbial attachment promoted Fe(ii) scavenging which outcompeted As(iii) from the available ligands in the reactive mineral surfaces. Improving mineral stabilization is deemed crucial for direct As(iii)-sequestration in BESs. An optimized BES for As-removal would be beneficial not only for sequestering arsenite out of solution in geogenically polluted aqueous systems, but also for addressing the recurrent eutrophication of continental water bodies linked to seasonal phosphate solubilization.

  • Název v anglickém jazyce

    Anaerobic dissolved As(III) removal from metalpolluted waters by cathode-stabilized Fe(III)- oxyhydroxides.

  • Popis výsledku anglicky

    A bioelectrochemical system (BES) to efficiently induce arsenite scavenging from anoxic waters is yet to be developed. Here we examined to what extent the presence of redox reactive humic substances derivatives and reactive nitrogen species interferes with the bioelectrochemically induced immobilization of As(iii) by Fe(iii) oxyhydroxides. Insights from extracellular electron transfer to insoluble minerals by a strain of Geobacter sp. were acquired and integrated with data from acetate utilization. We furthered our interpretations with in situ synchrotron-based analyses of experimentally precipitated biominerals. Geobacter sp. cells interacting with cathodes used oxidized humic substance derivatives as electron shuttles which fostered the partial reduction of Fe(iii), thus promoting the scavenging of As(iii) oxyanions. The oxyanions became immobilized in the reactive surfaces of FeOOH within mineral aggregates, where they were readily oxidized presumably as the result of related Fenton-like reactions. An experiment lacking humic derivatives fueled the formation of bacterial-mineral networks. These networks fostered short-range electron transfer mechanisms that initially promoted biotic amorphous ferrihydrite aggregation. The early ferrihydrite aggregates exhibited a decreased As(iii) scavenging capacity. In the presence of both humic derivatives and ammonium, the proposed BES was proven more effective in removing As(iii) from solution and despite elevated competing phosphate levels. In the presence of reactive N species alone, stabilization of Fe(iii) and microbial attachment promoted Fe(ii) scavenging which outcompeted As(iii) from the available ligands in the reactive mineral surfaces. Improving mineral stabilization is deemed crucial for direct As(iii)-sequestration in BESs. An optimized BES for As-removal would be beneficial not only for sequestering arsenite out of solution in geogenically polluted aqueous systems, but also for addressing the recurrent eutrophication of continental water bodies linked to seasonal phosphate solubilization.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10503 - Water resources

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/GJ19-15096Y" target="_blank" >GJ19-15096Y: Souběžné mikrobiálně řízené cykly železa, dusíku a fosforu a jejich přechodové oddělení v vodních ekosystémech bohatých na redukované železo</a><br>

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2023

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Environmental Science-Water Research & Technology

  • ISSN

    2053-1400

  • e-ISSN

    2053-1419

  • Svazek periodika

    9

  • Číslo periodika v rámci svazku

    2

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    13

  • Strana od-do

    454-466

  • Kód UT WoS článku

    000897894400001

  • EID výsledku v databázi Scopus

    2-s2.0-85144807061